There is provided an optical imaging device (18) for splitting an initial image into at least two images with different optical characteristics. The device comprises a dichroic mirror (32) to create first and second optical pathways respectively incident on first and second mirrors (41, 41′) carried on a centrally pivoted rotatable arm, characterised in that the first and second reflective means are moveable along the arm (42) whilst held in fixed relationship to each other, thereby to adjust separation of the first and second optical pathways. A third mirror (46) in fixed relationship to the beam splitter (32) is positioned adjacent where the first and second optical pathways intersect, or just before the intersection of the first and second optical pathways, or just after the point of intersection.
|
1. An optical imaging device for splitting an initial image into at least two images with different optical characteristics, wherein the device comprises a beam splitter to create first and second optical pathways respectively incident on first and second reflectors carried on a centrally pivoted rotatable arm, the first and second reflectors are moveable along the arm whilst held in fixed relationship to each other, thereby to adjust separation of the first and second optical pathways, and a third reflector in fixed relationship to the beam splitter is positioned to intersect the first and second optical pathways with the orientation of the third reflector adjustable dependent on whether an input beam of the device is to be parallel or at right angles to an output beam.
2. An optical imaging device according to
3. An optical imaging device according to
4. An optical imaging device according to
5. An optical imaging device according to
6. An optical imaging device according to
|
This invention relates to an optical imaging device, and in particular to a device capable of splitting a single optical image into further images.
Within complex optical systems, optical imaging devices are used for manipulation of an optical image. Devices which allow an image to be split into a plurality of images with different optical characteristics are often used within spectroscopes or spectral imagers. The different images have, for example, different wavelengths or different polarisations, and can be viewed simultaneously to give information about a sample being examined under a microscope.
Prior art devices used for producing the images with different optical characteristics are often complex, and can introduce optical aberrations which complicate assessment of the plurality of images.
It is an aim of the present invention to provide a simplified optical imaging device which essentially reduces optical aberrations.
In accordance with one aspect of the present invention, there is provided an optical imaging device for splitting an initial image into at least two images with different optical characteristics, wherein the device comprises a beam splitter to create first and second optical pathways respectively incident on first and second reflective means carried on a centrally pivoted rotatable arm, characterised in that the first and second reflective means are moveable along the arm whilst held in fixed relationship to each other, thereby to adjust separation of the first and second optical pathways. By having the first and second reflective means moveable along the arm, but yet the first and second reflective means remaining fixed relative to one another, the characteristics of the optics preceding the optical imaging device, for example a microscope in which the optical imaging device is placed so as to allow spectroscopic analysis, are no longer relevant to adjustment of the optical pathways.
The beam splitter will typically be a dichroic mirror which reflects a proportion of incident light whilst transmitting the remainder of the incident light. Other types of beam splitters which may be used include polarising beam splitters. The dichroic mirror may be coated so as to alter the optical characteristics of both, or either of, the reflected and transmitted light. Additional optical elements, such as filters, may be placed in the optical pathways.
Preferably the first and second reflective means are mirrors, which again may be provided with coatings or modified in other ways so as to alter the optical characteristics along the optical pathways. Movement of the first and second reflective means along the arm allows the position of the first optical pathway to be adjusted relative to the second optical pathway prior to recombination at an output. This allows adjustment of the optical pathways to match the preceding optics, and allows the first and second optical pathways to be placed as close together as possible whilst avoiding overlap.
Preferably a third reflective means, such as another mirror, in fixed relationship to the beam splitter is positioned adjacent where the first and second optical pathways intersect so as to deflect one, or the first, optical pathway to a first focussing element, such as a lens, for recombination with the other, or the second, optical pathway.
The third reflective means may be positioned just before the intersection of the first and second optical pathways, as shown in
Alternatively the third reflective means may be positioned just after the point of intersection, see
The orientation of the third reflective means may be adjusted dependent on whether an input beam to the device is to be parallel or at right angles to an output beam.
If desired the third reflective means may be omitted and first and second focussing elements used to focus the first and second optical pathways respectively, the pathways intersecting, but not recombining, before reaching their respective focussing elements.
The invention will now be described, by way of example, with reference to the accompanying drawings in which:
The optical system comprises a microscope 14 which includes an objective lens 16 for receiving light from the sample 12 so as to create an image, an optical imaging device 18 mounted on a microscope port and for splitting the image into two or more further images with different optical characteristics, and an imaging lens 20 for focussing these images on output to an image receiving surface 22 such as a solid state imaging device or a detector array.
As is known in the art, the transmission of light through any optical system is limited by the size of the various apertures within it. Some of these apertures are there by physical necessity, for example the finite diameters of various lenses and other optical components, and others are selected in order to give the system specific characteristics. An aperture may be used to limit a field of view, for example of a specimen that is being imaged. In order to do this, the aperture must be in focus when the image of the object is in focus: this is known as a field iris. An aperture may also be used to control the amount of light transmitted by the system and in microscopy this is known as a condenser iris on the illumination side, and an exit pupil on the light collection side. The condenser iris must not be in or near focus with the object. Whereas a field iris sets the lateral displacement from the optical axis (i.e. centre of field) over which the object can be seen, a condenser iris or exit pupil sets the range of angles over which light can be collected from the object and re-imaged.
In the system shown in
The images obtained by the microscope 14 are usually viewed at high magnification, with the effect of magnifying an image being to correspondingly reduce the range of angles that the imaging light subtends to the optical axis. Thus the greater the magnification, the more closely the image-forming light approximates to a parallel beam, and therefore the beam divergence becomes less with magnification. By keeping the overall path length through the splitter 18 as short as possible, and by using optical components of reasonably large diameter relative to the beam, the beam divergence remains below a diameter at which significant optical aberration occurs.
A prior art image splitter is shown in
Thus light from the image plane is collimated by lens 30, and then split into two essentially equal pathways by dichroic mirror 32 which is oriented slightly clockwise with respect to an exact 45° angle. The beam transmitted by dichroic mirror 32 is redirected by 45° mirror 35 and reflected by mirror 35″ towards the output focussing lens 36. The beam reflected by mirror 32 is reflected by 45° mirror 35′ and passes by the side of mirror 35″ to be focussed by lens 36. Separation of the two images at the output is effected by anticlockwise rotation of mirrors 35 and 35′. To achieve equal rotation, mirrors 35 and 35′ are mounted on a common carrier which rotates around a pivot 38. The rotation also physically separates the two beams at mirror 35″ so that the beam reflected from mirror 35 falls entirely on mirror 35″, whereas the beam reflected from mirror 35′ passes completely to the right of 35″.
The light reflected by dichroic mirror 32 arrives at mirror 35′ somewhat lower and to the right than the transmitted light arriving at mirror 35″, and mirrors 35 and 35′ are biased slightly clockwise to compensate. Mirror 35″ is also biased slightly clockwise to match the rotation of mirror 35. The effect of this is that even at zero image separation the two beams may not overlap at the position of mirror 35″. However the two beams should not be separated by more than necessary at mirror 35″, otherwise their centres will be further away from the optical axis of lens 36 than they need to be, which will require lens 36 to operate at a faster focal ratio, which will in turn increase the aberrations from lens 36. Image splitters are usually sold as add-on devices, and there is no way of knowing the characteristics of the optical system to which the splitter is going to be connected, even though the characteristics of the optical system will influence the beam diameters at the location of mirror 35″, and thus the required centre spacing. For example, one cannot predict where the exit pupil of an unknown optical device will be.
Where a microscope is operating at high magnifications, there are very long focal ratios and the collimated beams between lenses 30 and 36 will generally not diverge very much so reducing the possible problems with beam separation at mirror 35″.
However where magnification is not particularly high, the greater beam divergence between lenses 30 and 36 requires a greater beam separation within the splitter, so that optical pathway 33 is still entirely unobstructed by mirror 35″ and optical pathway 34 is still entirely reflected by it. In order to deal with worst-case conditions the beam separation at lens 36 may therefore be large enough for this lens to produce significant aberration, as the light pathways are further off-axis. An image splitter in accordance with the present invention, see
In the image splitter 40 of
Alternatively an arrangement as shown in
Two positions of mirrors 41 and 41′ are shown in
As the position of the carriage is adjustable to allow the optical pathways of the splitter to be altered to match the preceding optics, whose characteristics will always be unknown at point of sale, the dichroic mirror 32 is positioned at exactly 45°.
Ideally, the two beams are only separated by the minimum distance necessary to prevent overlap, which is simple to do given the ease of sliding the carriage relative to the axis 44. Also mirror 46 can have its reflective surface angled back at 45° at the edge closest to beam 33 so as to avoid any obstruction to beam 33. Too much separation will require lens 36 to operate at a faster focal ratio, so increasing aberrations from the lens, which is not desirable.
The splitter of
In
The direction of rotation is selected so as to increase the separation of the two beams at the half-length mirror 46, 46′, so as to require less linear displacement of mirrors 41, 41′. Whilst the preferred direction of rotation for the embodiment shown in
In the embodiments shown in
If required, adjustable iris diaphragms 48 are placed in the pathways from the beam splitter 32 to obstruct the beams and so allow the intensities of beams 33 and 34 to be adjusted independently. This is useful if one beam is significantly brighter than the other and allows the intensities of the beams to be adjusted to be approximately the same. This is particularly useful if both beams are being imaged at the same projector. The diaphragms 48 are ideally placed one focal length before the refocussing lens 36, so that they are completely out of focus at the final image.
Two or more of the embodiments shown may be combined, for example those shown in
As will be apparent to one skilled in the art, other optical elements can be used instead of mirrors, for example gratings, prisms, or polarisers. Optical elements such as filters, polarisers etc. can also be used in combination with the mirrors. For the arrangement shown in
The preceding optics, especially if working at high magnification such as a microscope, may introduce significant chromatic aberration. When image separation is carried out on the basis of wavelength, it may no longer be possible for both images to be in sharp focus. However, this situation can be alleviated by including corrector optics in the split pathways. In the configuration shown in
Patent | Priority | Assignee | Title |
10684459, | Jun 03 2013 | Hamamatsu Photonics K.K. | Light observation device, imaging device used for same, and light observation method |
7889263, | Oct 12 2000 | CYTEK BIOSCIENCES, INC | System and method for high numeric aperture imaging systems |
7925069, | Jan 25 1999 | CYTEK BIOSCIENCES, INC | Blood and cell analysis using an imaging flow cytometer |
8005314, | Dec 09 2005 | CYTEK BIOSCIENCES, INC | Extended depth of field imaging for high speed object analysis |
8103080, | Mar 16 2004 | CYTEK BIOSCIENCES, INC | Method for imaging and differential analysis of cells |
8131053, | Jan 25 1999 | CYTEK BIOSCIENCES, INC | Detection of circulating tumor cells using imaging flow cytometry |
8150136, | Mar 16 2005 | CYTEK BIOSCIENCES, INC | Image based quantitation of molecular translocation |
8379136, | Oct 12 2000 | CYTEK BIOSCIENCES, INC | System and method for high numeric aperture imaging systems |
8406498, | Jan 25 1999 | CYTEK BIOSCIENCES, INC | Blood and cell analysis using an imaging flow cytometer |
8451524, | Sep 29 2009 | CYTEK BIOSCIENCES, INC | Modifying the output of a laser to achieve a flat top in the laser's Gaussian beam intensity profile |
8548219, | Jan 25 1999 | CYTEK BIOSCIENCES, INC | Detection of circulating tumor cells using imaging flow cytometry |
8571294, | Mar 16 2004 | CYTEK BIOSCIENCES, INC | Method for imaging and differential analysis of cells |
8571295, | Mar 16 2004 | CYTEK BIOSCIENCES, INC | Method for imaging and differential analysis of cells |
8660332, | Jan 25 1999 | CYTEK BIOSCIENCES, INC | Blood and cell analysis using an imaging flow cytometer |
8817115, | May 05 2010 | CYTEK BIOSCIENCES, INC | Spatial alignment of image data from a multichannel detector using a reference image |
8824770, | Mar 16 2004 | CYTEK BIOSCIENCES, INC | Method for imaging and differential analysis of cells |
8885913, | Jan 25 1999 | CYTEK BIOSCIENCES, INC | Detection of circulating tumor cells using imaging flow cytometry |
8922896, | Nov 13 2012 | Cairn Research Limited | Optical imaging device |
8953866, | Mar 16 2004 | CYTEK BIOSCIENCES, INC | Method for imaging and differential analysis of cells |
9995920, | Jun 03 2013 | HAMAMATSU PHOTONICS K K | Light observation device, imaging device used for same, and light observation method |
Patent | Priority | Assignee | Title |
6814484, | Jul 01 2002 | NORITAKE CO , LIMITED; KITAGAWA, KUNIYUKI | Temperature distribution measuring method and apparatus |
6856459, | Dec 22 2000 | Cheetah Omni, LLC | Apparatus and method for controlling polarization of an optical signal |
GB2162334, |
Executed on | Assignor | Assignee | Conveyance | Frame | Reel | Doc |
Jun 27 2005 | Cairn Research Limited | (assignment on the face of the patent) | / | |||
Aug 10 2005 | THOMAS, MARTIN | Cairn Research Limited | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 016811 | /0423 |
Date | Maintenance Fee Events |
Jul 18 2013 | ASPN: Payor Number Assigned. |
Aug 16 2013 | M1551: Payment of Maintenance Fee, 4th Year, Large Entity. |
Aug 15 2017 | M1552: Payment of Maintenance Fee, 8th Year, Large Entity. |
Aug 16 2021 | M1553: Payment of Maintenance Fee, 12th Year, Large Entity. |
Date | Maintenance Schedule |
Feb 23 2013 | 4 years fee payment window open |
Aug 23 2013 | 6 months grace period start (w surcharge) |
Feb 23 2014 | patent expiry (for year 4) |
Feb 23 2016 | 2 years to revive unintentionally abandoned end. (for year 4) |
Feb 23 2017 | 8 years fee payment window open |
Aug 23 2017 | 6 months grace period start (w surcharge) |
Feb 23 2018 | patent expiry (for year 8) |
Feb 23 2020 | 2 years to revive unintentionally abandoned end. (for year 8) |
Feb 23 2021 | 12 years fee payment window open |
Aug 23 2021 | 6 months grace period start (w surcharge) |
Feb 23 2022 | patent expiry (for year 12) |
Feb 23 2024 | 2 years to revive unintentionally abandoned end. (for year 12) |